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Transient neonatal diabetes mellitus and activating mutation in the KCNJ11 gene in two siblings.
Kamoun, T; Chabchoub, I; Ben Ameur, S; Kmiha, S; Aloulou, H; Cave, H; Polak, M; Hachicha, M.
Affiliation
  • Kamoun T; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
  • Chabchoub I; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
  • Ben Ameur S; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia. Electronic address: benameursalma@gmail.com.
  • Kmiha S; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
  • Aloulou H; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
  • Cave H; Department of genetics, Robert-Debré university hospital, Assistance publique-Hôpitaux de Paris, 75019 Paris, France.
  • Polak M; Paediatric endocrine unit, centre of rare endocrine diseases of growth, Necker-Enfants-Malades hospital, AP-HP, 75012 Paris, France.
  • Hachicha M; Faculty of medicine Sfax, university of Sfax, Sfax, Tunisia; Service de pédiatrie, pediatric department, Hédi Chaker hospital, El Ain street K 0.5, 3029 Sfax, Tunisia.
Arch Pediatr ; 24(5): 453-456, 2017 May.
Article in En | MEDLINE | ID: mdl-28347637
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 6 / Potassium Channels, Inwardly Rectifying / Diabetes Mellitus / Genetic Carrier Screening / Infant, Newborn, Diseases Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Humans / Infant / Male / Newborn Language: En Journal: Arch Pediatr Year: 2017 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 6 / Potassium Channels, Inwardly Rectifying / Diabetes Mellitus / Genetic Carrier Screening / Infant, Newborn, Diseases Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Humans / Infant / Male / Newborn Language: En Journal: Arch Pediatr Year: 2017 Document type: Article Affiliation country: